化工社化工社 化学情報印刷レポート · 研究参考用
Hydrochloric Acid → Ethyl 7-bromoimidazo[1,2-a]pyridine-3-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 1,4-Dioxane | HCID 31275 | — |
| 反応物 | 2-Amino-4-bromopyridine | HCID 693282 | — |
| 反応物 | Potassium (E)-2-chloro-3-ethoxy-3-oxoprop-1-en-1-olate | HCID 23711836 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Ethyl 7-bromoimidazo[1,2-a]pyridine-3-carboxylate | HCID 67260906 | 74.3% |
反応手順
Potassium (E)-2-chloro-3-ethoxy-3-oxoprop-1-en-1-olate (4.4 g, 23 mmol; prepared as in Example 65, step B1) was suspended in toluene (40 mL) and a 4M solution of HCl in dioxane (2.0 mL, 8.1 mmol). The mixture was stirred at ambient temperature for 5 minutes. 4-Bromopyridin-2-amine (2.0 g, 12 mmol) was added to the mixture and heated to 40° C. for 22 hours. The mixture was cooled to ambient temperature and extracted with 2M HCl (3×75 mL). Solid K2CO3 was added to the combined aqueous extracts until CO2 evolution ceased. The aqueous phase was extracted with MTBE (2×50 mL), dried over MgSO4, filtered and concentrated to give the product (2.4 g). MS (ES+APCI) m/z=268.7 (M+H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08841455B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-78e23bd9e68a406c9c5de6f9f892a1c3 |
| 出典メモ | uspto-grants-2014_09 |